ETV2 null porcine embryos survive to post-implantation following incomplete enucleation

Geunho Maeng, Wuming Gong, Satyabrata Das, Demetris Yannopoulous, Daniel Garry, Mary Grace Garry

Research output: Contribution to journalArticlepeer-review

3 Scopus citations


Blind enucleation is used in porcine Somatic Cell Nuclear Transfer (SCNT) to remove the metaphase II (MII) spindle from the oocyte. Deviation of the MII spindle location, however, leads to incomplete enucleation (IE). Here, we report that the rate of complete enucleation (CE) using the blind method was 80.2% ± 1.7%, although this significantly increased when the polar body-MII deviation was minimized (≦ 45°). While it is established that IE embryos will not survive to full term, the effect of IE on early stage development is unknown. We have previously demonstrated in mice and pigs that ETV2 deletion results in embryonic lethality due to the lack of hematoendothelial lineages. We observed that ETV2-null cloned embryos derived from blindly and incompletely enucleated oocytes had both WT and mutant sequences at E18 and, using FISH analysis, we observed triploidy. We also compared SCNT embryos generated from either CE or intentionally IE oocytes using the spindle viewer system. We observed a higher in vitro blastocyst rate in the IE versus the CE-SCNT embryos (31.9 ± 3.2% vs. 21.0 ± 2.1%). Based on known processes in normal fertilization, we infer that the IE-SCNT embryos extruded the haploid second PB after fusion with donor fibroblasts and formed a near-triploid aneuploid nucleus in each blastomere. These studies demonstrate the peri-implantation survival of residual haploid nuclei following IE, and emphasize the need for complete enucleation especially for the analysis of SCNT embryos in the peri-implantation stage and will, further, impact the field of reverse xenotransplantation.

Original languageEnglish (US)
Pages (from-to)539-547
Number of pages9
Issue number5
StatePublished - May 2020

Bibliographical note

Funding Information:
This work was supported by the American Heart Association (grant number 18TPA34220008).

Publisher Copyright:
© 2020 Society for Reproduction and Fertility.

PubMed: MeSH publication types

  • Journal Article
  • Research Support, Non-U.S. Gov't


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